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Regulatory Affairs Mgr

3+ years
₹40–55 LPA
10 July 6, 2025
Job Description
Job Type: Full Time Education: PhD/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regulatory Affairs Manager
Location: Hyderabad, India
Job ID: R-215832
Posted On: June 04, 2025
Employment Type: Full-Time | On-Site

About Amgen:
Amgen is a global pioneer in biotechnology, committed to unlocking the potential of biology for patients suffering from serious illnesses. With over 40 years of experience, Amgen remains at the forefront of scientific innovation, addressing complex diseases in Oncology, Inflammation, General Medicine, and Rare Disease.


Role Overview:

As the International Regulatory Lead (IRL) Manager, you will provide strategic regulatory leadership for one or more products within Amgen’s portfolio. This role supports the development and execution of regulatory strategies to ensure successful product development, registration, and lifecycle management in international markets. You will serve as a key liaison between global functions and local regulatory teams, driving alignment and ensuring compliance with regulatory requirements.


Key Responsibilities:

Strategic Regulatory Planning:

  • Advise global teams on international regulatory requirements and strategies for product development and approvals.

  • Develop and execute international regulatory strategies, including regulatory product filing plans, risk assessments, and contingency plans.

  • Coordinate global clinical development strategies with regional submission timelines and objectives.

Submission & Lifecycle Management:

  • Plan and manage regulatory submissions for clinical trials, marketing authorizations, and post-approval changes.

  • Contribute to the development and maintenance of application documentation, excluding CMC components.

  • Lead international labeling strategy, including deviation negotiations and submission alignment.

Cross-Functional Collaboration:

  • Act as a member of the Global Regulatory Team (GRT) and collaborate with global clinical and labeling teams.

  • Liaise regularly with local regulatory affiliates to ensure strategy alignment and share development updates.

  • Support query triaging and knowledge sharing across teams for efficient health authority interactions.

Monitoring & Compliance:

  • Stay informed on global regulatory developments, policy changes, and technical guidance.

  • Conduct regulatory research and maintain awareness of international legislative changes that impact Amgen’s pipeline and marketed products.


Required Qualifications:

  • Doctorate degree
    OR

  • Master’s degree with 3 years of relevant regional regulatory experience
    OR

  • Bachelor’s degree with 5 years of relevant regional regulatory experience
    OR

  • Associate degree with 10 years of relevant experience
    OR

  • High school diploma/GED with 12 years of relevant experience


Functional & Technical Skills:

Must-Have:

  • Experience in regulatory environments relevant to clinical trials, marketing authorizations, and labeling activities.

  • Solid understanding of regulatory frameworks in biotechnology, particularly in oncology or other therapeutic areas.

  • Knowledge of international submission processes and lifecycle management challenges.

Good-to-Have:

  • Conflict resolution skills with the ability to navigate complex regulatory scenarios.

  • Cultural sensitivity and experience working across global teams and regional regulations.


Soft Skills:

  • Strong oral and written communication, especially in conveying scientific and regulatory information.

  • Highly organized, self-motivated, and capable of managing multiple priorities.

  • Team-oriented mindset with effective negotiation and influencing abilities.


Estimated Salary: ₹40–55 LPA (based on market benchmarks for regulatory leadership roles)